CHF19.00
The Medical Device Regulation MDR 2017/745, Annex I, 23.4, defines the content requirements for Instructions for Use (IFU) for medical devices. The information to be supplied in the IFU is crucial for the communication of safety, effectiveness and correct use to the user. Find here the checklist for the IFU content, delivered as:
The MDR 2017/745 defines in its Annex I, 23.4 the content requirements for the information in the Instructions for Use (IFU) for medical devices. Find here the checklist and supportive information to correctly establish an IFU for medical devices.
